FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

VITROS IMMUNODIAGNOSTICS PRODUCTS FREE T4 REAGENT PACK (GEM.1015) FREE T4 CALIBRATORS (GEM.CO15)

K Number: K965142 · Decision Mar 18, 1997
Classifications
1
FEI Numbers
43
Registration Numbers
43
Same Product Code
91
Applicant Total
33
Review Days
85

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Basic Information

Device Name
VITROS IMMUNODIAGNOSTICS PRODUCTS FREE T4 REAGENT PACK (GEM.1015) FREE T4 CALIBRATORS (GEM.CO15)
K Number
K965142
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1695
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Johnson & Johnson Clinical Diagnostics, Inc.
Date Received
December 23, 1996
Decision Date
March 18, 1997
Product Code
CEC
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
CEC Radioimmunoassay, Free Thyroxine

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Other Clearances by Johnson & Johnson Clinical Diagnostics, Inc.

K Number Device Name
K980283 VITROS CHEMISTRY PRODUCTS CRBM SLIDES
K974644 VITROS IMMUNODIAGNOSTIC PRODUCTS RANGE VERIFIERS
K973517 VITROS IMMUNODIAGNOSTIC PRODUCTS RANGE VERIFIERS
K973030 VITROS IMMUNODIAGNOSTICS PRODUCTS/CK-MB REAGENT PACK(GEM.1300)/CK-MB CALIBRATORS (GEM.C300)
K972133 VITROS IMMUNODIAGNOSTICS PRODUCTS PROGESTERONE REAGENT PACK (GEM.1070), PROGESTERONE CALIBRATORS (GEM.C070)
K970894 VITROS IMMUNODIAGNOSTICS PRODUCTS TOTAL B-HCG REAGENT PACK (GEM.1075), TOTAL B-HCG CALIBRATORS (GEM.C075)
K970643 VITROS IMMUNODIAGNOSTICS PRODUCTS ESTRADIOL REAGENT PACK(GEM. 1050)/ESTRADIOL CALIBRATORS (GEM.C050)
K970281 VITROS IMMUNODIAGNOSTIC PRODUCTS PROLACTIN REAGENT PACK/CALIBRATORS
K964982 VITROS IMMUNODIAGNOSTICS PRODUCTS LH REAGENT PACK (GEM.1055) AND LH CALIBRATORS (GEM.CO55)
K964960 VITROS CHEMISTRY PRODUCTS UPRO SLIDES
Search all 33 clearances from Johnson & Johnson Clinical Diagnostics, Inc. →